Cas 98965-59-4,<4,4-Dimethyl-3-methylen-1-<4-(4-methylphenyl)-3,5-dioxo-1,2,4-triazolidin-1-yl>-1-pentenyl>phosphonsaeure-dimethylester

98965-59-4

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Basic information

Product Name: <4,4-Dimethyl-3-methylen-1-<4-(4-methylphenyl)-3,5-dioxo-1,2,4-triazolidin-1-yl>-1-pentenyl>phosphonsaeure-dimethylester
Synonyms:
CAS NO:98965-59-4
Molecular Formula:
Molecular Weight: 407.406
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: <4,4-Dimethyl-3-methylen-1-<4-(4-methylphenyl)-3,5-dioxo-1,2,4-triazolidin-1-yl>-1-pentenyl>phosphonsaeure-dimethylester(CAS DataBase Reference)
NIST Chemistry Reference: <4,4-Dimethyl-3-methylen-1-<4-(4-methylphenyl)-3,5-dioxo-1,2,4-triazolidin-1-yl>-1-pentenyl>phosphonsaeure-dimethylester(98965-59-4)
EPA Substance Registry System: <4,4-Dimethyl-3-methylen-1-<4-(4-methylphenyl)-3,5-dioxo-1,2,4-triazolidin-1-yl>-1-pentenyl>phosphonsaeure-dimethylester(98965-59-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 98965-59-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98965-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,9,6 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98965-59:
(7*9)+(6*8)+(5*9)+(4*6)+(3*5)+(2*5)+(1*9)=214
214 % 10 = 4
So 98965-59-4 is a valid CAS Registry Number.

98965-59-4Upstream product

72708-83-9 4-(4-Methylphenyl)-1,2,4-triazoline-3,5-dione

98965-59-4Downstream Products

98965-59-4Relevant academic research and scientific papers

Investigations on Diazo Compounds and Azides, LX. Reactions of 3H-1,2,4-Triazole-3,5(4H)-diones with Vinyl Diazo Compounds

Theis, Wolfgang,Regitz, Manfred

, p. 3396 - 3407 (2007/10/02)

Vinyl diazo compounds react with triazolediones depending on the substitution pattern and the reaction conditions either at the carbon double bond or at the diazo carbon atom.Thus from 10a and d and 2a-c in dichloromethane/ethanol the new diazo compounds

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